AFFIXUS®HIP FRACTURE NAIL LAG SCREW 8145-10-110Recalls & reported problems
Biomet Orthopedics, LLC · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00887868039041), received between Mar 18, 2024 and Mar 18, 2024 — classified as 1 injury.
The most frequently reported specific device problem is “Migration” (1 report).
250 other recalls cover devices cleared under the same FDA submission (K100238); they may or may not involve this specific model.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Reports received per month
Most reported problems
Device problems
- Migration1
- Patient Device Interaction Problem1
Patient problems
- Discomfort1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryMar 18, 2024Patient Device Interaction Problem; Migration; Patient Device Interaction Problem; Migration
IT WAS REPORTED THAT THE PATIENT UNDERWENT AN INITIAL HIP FRACTURE SURGERY APPROXIMATELY SEVEN (7) YEARS AGO, SUBSEQUENTLY, THE PATIENT IS ABLE TO PALPATE THE LAG SCREW THROUGH THE SKIN AND THIS IS CAUSING THE PATIENT DISCOMFORT. THE SURGEON HAS RECOMMENDED THAT THE SCREW BE EXPLANTED FROM THE PATIENT. A REVISION SURGERY HAS NOT BEEN SCHEDULED. MULTIPLE ATTEMPTS HAVE BEEN MADE TO OBTAIN ADDITIONAL INFORMATION, BUT NO RESPONSE HAS BEEN RECEIVED.
Patient problems: Discomfort
MAUDE report 18924090 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K100238. One submission often covers many models, so check the product and lot details in each record.
- Z-0449-2019 · Oct 2, 2018 · TerminatedAffixus Hip Fracture Nail Left 130 Deg 11x300mm, Item Number 814611300 The Affixus Hip Fracture Nail System, comprised of short and long nails, provides surgeons with an intramed
- Z-0453-2019 · Oct 2, 2018 · TerminatedAffixus Hip Fracture Nail 130 Deg 10x165mm, Item Number 816810165 The Affixus Hip Fracture Nail System, comprised of short and long nails, provides surgeons with an intramedullar
- Z-0448-2019 · Oct 2, 2018 · TerminatedAffixus Hip Fracture Nail Left 125 Deg 11x300mm, Item Number 814411300 The Affixus Hip Fracture Nail System, comprised of short and long nails, provides surgeons with an intramed
- Z-0447-2019 · Oct 2, 2018 · TerminatedAffixus Hip Fracture Nail Left Deg 9x300mm, Item Number 814609300 The Affixus Hip Fracture Nail System, comprised of short and long nails, provides surgeons with an intramedullar
- Z-0452-2019 · Oct 2, 2018 · TerminatedAffixus Hip Fracture Nail 125 Deg 12x165mm, Item Number 816712165 The Affixus Hip Fracture Nail System, comprised of short and long nails, provides surgeons with an intramedullar
- Z-0451-2019 · Oct 2, 2018 · TerminatedAffixus Hip Fracture Nail 125 Deg 10x165mm, Item Number 816710165 The Affixus Hip Fracture Nail System, comprised of short and long nails, provides surgeons with an intramedullar
- Z-0450-2019 · Oct 2, 2018 · TerminatedAffixus Hip Fracture Nail Left 125 Deg 9x165mm, Item Number 816709165 The Affixus Hip Fracture Nail System, comprised of short and long nails, provides surgeons with an intramedu
- Z-0454-2019 · Oct 2, 2018 · TerminatedAffixus Hip Fracture Nail 130 Deg 12x165mm, Item Number 816812165 The Affixus Hip Fracture Nail System, comprised of short and long nails, provides surgeons with an intramedullar
- Z-0131-2019 · Aug 8, 2018 · TerminatedAffixus Hip Fracture Nail 125 11mm x 180mm, Item Number 814311180 Product Usage: Intended for the fixation of fractures
- Z-0133-2019 · Aug 8, 2018 · TerminatedAffixus Hip Fracture Nail Right 125 11 mm x 360 mm, Item Number 814311360 Product Usage: Intended for the fixation of fractures
- Z-0168-2019 · Aug 8, 2018 · TerminatedAffixus Hip Fracture Nail Left 130 15 mm x 360 mm, Item Number 814615360 Product Usage: Intended for the fixation of fractures
- Z-0140-2019 · Aug 8, 2018 · TerminatedAffixus Hip Fracture Nail Right 125 13 mm x 280 mm, Item Number 814313280 Product Usage: Intended for the fixation of fractures
- Z-0154-2019 · Aug 8, 2018 · TerminatedAffixus Hip Fracture Nail Left 125 13 mm x 260 mm, Item Number 814413260 Product Usage: Intended for the fixation of fractures
- Z-0169-2019 · Aug 8, 2018 · TerminatedAffixus Hip Fracture Nail 125 9 mm x 165 mm, Item Number 816709165 Product Usage: Intended for the fixation of fractures
- Z-0134-2019 · Aug 8, 2018 · TerminatedAffixus Hip Fracture Nail Right 125 11 mm x 380 mm, Item Number 814311380 Product Usage: Intended for the fixation of fractures
…and 235 more.
Other ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES devices
- NA 03.033.001Synthes GmbH · ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES265 reports
- GAMMA 3125-1180SStryker GmbH · ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES249 reports
- NA 03.037.026Synthes GmbH · ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES225 reports
- PRECICE® Intramedullary Limb Lengthening System LSC5-075Nuvasive Specialized Orthopedics, Inc. · Rod, Fixation, Intramedullary And Accessories4 recalls2 reports
- PRECICE® Intramedullary Limb Lengthening System LSC5-045Nuvasive Specialized Orthopedics, Inc. · Rod, Fixation, Intramedullary And Accessories4 recalls1 report
- PRECICE® Intramedullary Limb Lengthening System LSC5-050Nuvasive Specialized Orthopedics, Inc. · Rod, Fixation, Intramedullary And Accessories4 recalls1 report
- TRIGEN 71674067Smith & Nephew, Inc. · ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES201 reports
- PRECICE Intramedullary Limb Lengthening System LSB5-040Nuvasive Specialized Orthopedics, Inc. · Rod, Fixation, Intramedullary And Accessories4 recalls0 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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